HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → diethyl O-[4-(2-cyclohexylethylamino)phenylacetyl]tartrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Butanedioic acid, 2,3-dihydroxy-, diethyl ester, S-(R*,R*)- | HCID 62333 | — |
| Reactant | 4-[N-trifluoroacetyl-(2-cyclohexylethylamino)]phenylacetyl chloride | HCID 20499025 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | diethyl O-[4-(2-cyclohexylethylamino)phenylacetyl]tartrate | HCID 20498970 | — |
Reaction Steps
A mixture of 4-[N-trifluoroacetyl-(2-cyclohexylethylamino)]phenylacetyl chloride and 1.2 g. triethylamine in 100 ml. warm ether is treated with 2.5 g. diethyl tartrate and refluxed for 24 hours. The hot solution is filtered, the residue is washed with hot ether, and the solution is evaporated. After treatment with aqueous methanolic potassium carbonate, the product is precipitated by acidification, filtered, and dried. Crystallization from acetone yields diethyl O-[4-(2-cyclohexylethylamino)phenylacetyl]tartrate as a white, crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04388459 |
| Source dataset | uspto-grants-1983_06 |
| ORD ID | ord-d923a3e2433141418e50e09b429ac3bf |
| Source note | uspto-grants-1983_06 |